Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and CRTAP[original query] |
|---|
| Next-generation sequencing of common osteogenesis imperfecta-related genes in clinical practice. Scientific reports 2016 6 28417. Árvai Kristóf, Horváth Péter, Balla Bernadett, Tobiás Bálint, Kató Karina, Kirschner Gyöngyi, Klujber Valéria, Lakatos Péter, Kósa János |
| Osteogenesis imperfecta in Brazilian patients. Genetics and molecular biology 2019 8 42 (2): 344-350. Trancozo Maira, Moraes Marcos V D, Silva Dalila A, Soares Jéssica A M, Barbirato Clara, Almeida Márcio G, Santos Lígia R, Rebouças Maria R G O, Akel Akel N, Sipolatti Valentim, Nunes Vanda R R, Errera Flavia I V, Aguena Meire, Passos-Bueno Maria R, Paula Flavia |
| On the association between Chiari malformation type 1, bone mineral density and bone related genes. Bone reports 2022 3 16 101181. Martínez-Gil Núria, Mellibovsky Leonardo, Manzano-López González Demián, Patiño Juan David, Cozar Monica, Rabionet Raquel, Grinberg Daniel, Balcells Susan |
- Page last reviewed:Feb 1, 2024
- Content source:

